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Methyl phenyl phosphorochloridothionate, also known as methyl phenyl phosphorodichloridothionate, is an organophosphorus compound with the chemical formula C7H7Cl2OPS. It is a colorless to pale yellow liquid with a pungent odor and is used as an intermediate in the synthesis of various pesticides, particularly organophosphorus insecticides. Methyl phenyl phosphorochloridothionate is highly toxic and can pose serious health risks if not handled properly, as it can cause severe damage to the nervous system. Due to its potential hazards, it is crucial to follow strict safety protocols when working with methyl phenyl phosphorochloridothionate.

6460-44-2

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6460-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6460-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6460-44:
(6*6)+(5*4)+(4*6)+(3*0)+(2*4)+(1*4)=92
92 % 10 = 2
So 6460-44-2 is a valid CAS Registry Number.

6460-44-2Relevant academic research and scientific papers

Kinetics and mechanism of pyridinolyses of aryl methyl and aryl propyl chlorothiophosphates in acetonitrile

Barai, Hasi Rani,Lee, Hai Whang

, p. 483 - 488 (2014/03/21)

The nucleophilic substitution reactions of Y-aryl methyl (8) and Y-aryl propyl (10) chlorothiophosphates with X-pyridines are studied kinetically in acetonitrile at 35.0 °C. The Hammett and Broensted plots with X in the nucleophiles for both substrates ex

A new convenient synthesis of phosphoro(-no)chloridothionates

He, Zheng-Jie,Liu, Ju-Xiang,Tang, Chu-Chi

, p. 2769 - 2772 (2007/10/03)

A general procedure for synthesis of phosphoro(-no)chlorides, particularly unsymmetrical ones, has been developed. The method involves the dealkylation of O,O-dialkyl phosphoro(-no)thionates 1 with dimethylamine and the chlorination of O-alkyl ammonium phosphoro(-no)thioates 2 using phosphorus oxychloride as a chlorinating agent.

Stereochemistry of Aryl Methyl Phosphorochloridothionates as Chiral Two-step Phosphorylating Reagents

Shao-Yong, Wu,Eto, Morifusa

, p. 3071 - 3080 (2007/10/02)

Seven aryl methyl phosphorochloridothionates were prepared and examined for reactivity as two-step phosphorylating reagents to synthesize oxazaphospholidine sulfide.The 2,6-dichloro-4-methylphenyl and p-nitrophenyl derivatives (CMPC and MNPC) were selecte

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